Code of Federal Regulations · Subchapter
Subchapter H — Medical Devices
21 C.F.R. subch. H
- Part 800 General
- Part 801 Labeling
- Part 803 Medical Device Reporting
- Part 806 Medical Devices; Reports Of Corrections And Removals
- Part 807 Establishment Registration And Device Listing For Manufacturers And Initial Importers Of Devices
- Part 808 Exemptions From Federal Preemption Of State And Local Medical Device Requirements
- Part 809 In Vitro Diagnostic Products For Human Use
- Part 810 Medical Device Recall Authority
- Part 812 Investigational Device Exemptions
- Part 813 Part 813 [reserved]
- Part 814 Premarket Approval Of Medical Devices
- Part 820 Quality Management System Regulation
- Part 821 Medical Device Tracking Requirements
- Part 822 Postmarket Surveillance
- Part 830 Unique Device Identification
- Part 860 Medical Device Classification Procedures
- Part 861 Procedures For Performance Standards Development
- Part 862 Clinical Chemistry And Clinical Toxicology Devices
- Part 864 Hematology And Pathology Devices
- Part 866 Immunology And Microbiology Devices
- Part 868 Anesthesiology Devices
- Part 870 Cardiovascular Devices
- Part 872 Dental Devices
- Part 874 Ear, Nose, And Throat Devices
- Part 876 Gastroenterology-urology Devices
- Part 878 General And Plastic Surgery Devices
- Part 880 General Hospital And Personal Use Devices
- Part 882 Neurological Devices
- Part 884 Obstetrical And Gynecological Devices
- Part 886 Ophthalmic Devices
- Part 888 Orthopedic Devices
- Part 890 Physical Medicine Devices
- Part 892 Radiology Devices
- Part 895 Banned Devices
- Part 898 Performance Standard For Electrode Lead Wires And Patient Cables